What happens next in GLP-1 — and when.

Get the briefing

What moved in the GLP‑1 field, in your inbox.

@glp1briefing

Trial results

Study Comparing the Efficacy and Safety of Insulin Glargine (Basal Insulin)/Lixisenatide (GLP-1 Receptor Agonist) Combination (Soliqua™) in Patients With Type 2 Diabetes Mellitus (T2DM)

NCT03767543 on ClinicalTrials.gov · last registry update 2022-04-25

Finished 23 October 2020, after enrolling 265 people. Primary outcome, as filed: Change in glycated hemoglobin (HbA1c)%. lixisenatide is already approved in the US for type 2 diabetes, so this is asking a further question rather than establishing the drug works at all. The registry entry has been edited 1 time since then.

Status
COMPLETED
Phase
P3
Drug
lixisenatide
Soliqua, Adlyxin
Sponsor
Sanofi
Sponsor type
Industry
Enrollment
265
Started
2019-03-11
Primary completion
2020-10-23 actual

Observed history

Every change this record has made since we started watching it. ClinicalTrials.gov shows only the current value. When a field is edited the previous one is overwritten and nothing is published to say so, so this history exists only because someone was recording it at the time.

DetectedChangeDetail
2026-08-21First seen in registryRegistered as COMPLETED, P3

Primary outcome

Change in glycated hemoglobin (HbA1c)%

Conditions studied

Type 2 Diabetes Mellitus

Every field above is taken directly from the registry record. See all detected changes across the class, or the lixisenatide page for this molecule’s full trial and approval history.